ECKER LAB PROTOCOL. Nested PCR and Sequencing of T-DNA Junctions in Arabidopsis

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1 ECKER LAB PROTOCOL Nested PCR and Sequencing of T-DNA Junctions in Arabidopsis Plant Growth Conditions The germination and DNA extraction of individual lines are done in 96-deep-well plates (Doc Frugal # or Beckman with corresponding lids). For the plate lid, punch holes with a needle in every well except those on the edge. A metal spoon was created to scoop about 30 seeds from an independent T2 plant line. Seeds were plated starting at position A1 and moving down the plate, then across (A1 to H1, then A2 to H2, etc.). Seed plates and lids are first gas-sterilized using bleach-hcl (25 ml bleach and 1 ml HCl) in a 5-liter hermetic chamber placed inside a fume hood. Keep the seed plates and lids in the gas for 30 minutes, then take them out and leave them (plates open) in a sterile hood overnight. Pour twenty milliliters of 0.5x MS salt solution (Gibco # ) containing diluted Daconil2787 (Ortho) [3 ml of 100 ml daconil/50 ml H 2 O stock per 20 ml media] and 60 ml 10 mm Gibberellic Acid (Sigma #G-7645) into a sterile petri dish. Add 60 ml of this solution to each well of the seed plate. Spin the plate(s) to 1500x g then stop. Keep the plates at 4 o C for three days. Remove the plates from the cold and transfer them to a clean growth chamber set for constant light and a temperature of 25 o C. Allow seedlings to grow about 6-8 days, then transfer the plates to the dark for another 3 days. I. Genomic DNA Prep Fill the lid of a 96-well plate (CLP #2407 or Beckman #267002) with a layer of 2.5mm zirconia/silica beads (Biospec Products # z). Remove extra beads by tilting the lid to 45 degrees. The wells should contain 1-3 beads each. Put the plate with the germinated seedlings in an inverted position on top of the lid, making sure that the holes of the plate and lid are aligned. Invert the plate and lid so the beads fall into the wells. The extraction protocol uses the Wizard 96 well magnetic bead system for plants (Promega #FF3761). 1) For 1 96-well plate mix 15 ml Lysis buffer A with 75 ml RNAse A (4mg/ml). RNA from the plant tissue may compete with DNA for the magnetic beads. 2) Add 150 ml of Lysis Buffer A to each well of the 96 well plate. 3) Seal the plates tightly with two layers of aluminum foil tape. 4) Grind the seedlings 2.5 minutes in a Harbil 5G-HD Mixer (Fluid Management) 5) Centrifuge plates 10 minutes at 2700x g and 4 o C 6) Carefully transfer 125ml of lysate to a new U bottom 96-well microtiter plate, making sure not to disturb the pellet. 7) Premix 5280 ml of Lysis Buffer B with 820 ml of resuspended Magnesil particles. 8) Add 60ml of Lysis B/Magnesil mix to the 125 ml of cell lysate. 9) Mix the plate to allow the DNA to bind to the Magnesil. This can be done using an eight-channel pipette for each well, or cover the plate very carefully with clear adhesive cover (ScotchPad from 3M), vortex and centrifuge (quick spin). Place the plate on the Magnabot and remove the supernatant. 10) Remove the plate from the Magnabot and add 100 ml of Wash Solution to each of the DNA/Magnesil wells. Mix the beads in the wash either by pipetting a few times per well, or carefully covering the plates with the adhesive cover and vortex then centrifuge. Place the plate

2 on the Magnabot. Invert plate over sink and place paper towel under the plate to soak up remaining wash solution. Repeat wash again using 100 ml of Wash Solution. If the wash still contains green color perform a third wash. After wash is complete, let the DNA/Magnesil dry at 37 o C until the beads are slightly moist and alchol has evaporated. Resuspend in 40 ml of 10 mm Tris, ph 8.3 for 15 minutes to overnight. 11) Place the plate on the Magnabot and transfer the DNA solution to a new plate. Run 1 ml from row C and F (columns 3 to 10) on a gel to check quality. II. Genomic Digest-Adaptor Ligation Adaptor Primers: LongAd: 5 GTA ATA CGA CTC ACT ATA GGG CAC GCG TGG TCG ACG GCC CGG GCT GC 3 ShortHind: 5 P-AGC TGC AGC CCG-NH2 3 * ShortEco: 5 P-AAT TGC AGC CCG-NH2 3 * ShortAse: 5 P-TAG CAG CCC G-NH2 3 * If the above Ase adaptor doesn t work well, use the following primers to make the adaptor: LongAdv.2: 5 GTA ATA CGA CTC ACT ATA GGG CAC GCG TGG TCG ACG GCC CGG GCT GTG C 3 ShortAsev.2: 5 P-TAG CAC AGC CCG-NH2 3 * *Note: the 5 Phosphate and 3 C7 amino mod. These primers are HPLC purified. When primers are obtained from Operon they arrive lyophilized. A data sheet is included. On the data sheet is the number of pmol of primer. Divide this number by 200 pmol/ml (this will be the final concentration) to determine the volume of water (or 10 mm Tris, ph 8.3) to add to the stock tube. Here is an example: Seq Name Seq 5 to 3 OD pmol Len MW ug Tm Scale Purif. ShortHind umol HPLC ShortEco umol HPLC ShortAse umol HPLC LongAd umol HPLC ShortHind: pmol / 200 pmol/ml = 284 ml of H 2 O to stock tube ShortEco : pmol / 200 pmol/ml = 275 ml of H 2 O to stock tube ShortAse : pmol / 200 pmol/ml = ml of H 2 O to stock tube LongAd : pmol / 200 pmol/ml = 529 ml of H 2 O to stock tube To make the adaptor, add to a small eppendorf tube: Hind Adaptor Eco Adaptor 82.5 ml NanoPure H 2 O 81.5 ml NanoPure H 2 O 10 ml 10mM Tris, ph ml 10mM Tris, ph ml 200 pmol LongAd primer 3.5 ml 200 pmol LongAd primer 4.0 ml 200 pmol ShortHind primer 5.0 ml 200 pmol ShortEco primer Ase Adaptor Ase Adaptor v ml NanoPure H 2 O 85 ml NanoPure H 2 O 10 ml 10mM Tris, ph ml 10mM Tris, ph 8.3

3 3.5 ml 200 pmol LongAd primer 3.5 ml 200 pmol LongAd primer 2.0 ml 200 pmol ShortAse primer 1.5 ml 200 pmol ShortAse primer Vortex and place tube on a wet heat block 96 o C for 2 minutes, then turn power off to heat block and remove the block from the heat mantle. Let cool to room temperature. Note: This method sometimes fails to work when a new stock is tested. This may be a result of incorrect DNA concentration, impure primers, etc. Always have some good primer stock stored so that new stocks can be compared to the primer standard. Primers can be compared via spec. and/ or gel electrophoresis. The volume of primer stocks used to make the adaptor may be modified as required. The Hind/Eco digestion and ligation steps are performed at the same time. For one 96-well PCR plate prepare the following: 550 ml MilliQ H 2 O or similar PCR quality water 100 ml NEB Ligase Buffer 25 ml Hind Adaptor 25 ml Eco Adaptor 10 ml NEB HindIII (2 U/rxn) 10 ml NEB EcoRI (2 U/rxn) 5 ml NEB T4 DNA Ligase (20 U/rxn) 5 ml 10 mm ATP Add 7 ml of mix to each well. Add ~100 ng of Genomic DNA to each reaction (2-3 microliters of the Magnesil DNA prep). Incubate overnight at room temperature. The AseI digest and ligation steps are performed separately. Digest for one 96-well plate: 250 ml MilliQ H 2 O or similar PCR quality water 60 ml Ligase buffer 20 ml Ase I (2 U/rxn) Add 3.5 ml Digest mix to well Add 2.5 ml DNA Digest 4 hours at 37 o C Ligation for one 96-well digest: 275 ml MilliQ H 2 O or similar PCR quality water 40 ml Ligase buffer 70 ml AseI Adaptor 12 ml 10 mm ATP 17 ml T4 DNA Ligase Add 4 ml Ligation mix to well

4 Incubate 20 o C overnight III. PCR PCR1 Primers: T-DNA Left Border a1 (Lba1): 5 TGG TTC ACG TAG TGG GCC ATC G 3 Adaptor Primer (AP1): 5 GTA ATA CGA CTC ACT ATA GGG C 3 PCR2 Primers: T-DNA Left Border b1 (LBb1): 5 GCG TGG ACC GCT TGC TGC AAC T 3 Adaptor Primer (AP2-C): 5 TGG TCG ACG GCC CGG GCT GC 3 PCR1: This protocol uses TaKaRa ExTaq and dntps. For one 96-well PCR plate prepare 1 tube of the following: 1650 ml MilliQ H 2 O or similar PCR quality water 200 ml 10x ExTaq PCR Buffer 80 ml 10 mm dntps 3 ml 200 pmol LBa1 primer (4 ml of 6/12/03 stock) 3 ml 200 pmol AP1 primer (4 ml of 6/12/03 stock) 6 ml ExTaq Pipette 20 ml of mix into each well of a 96-well PCR plate. Add 1 ml of ligated Hind/Eco DNA (1.5 ml ligated Ase DNA) to each reaction. Cover with rubber mat and immediately load on MJ paused at the initial 96 o C step. Cycle on an MJ-200 Thermal Cycler with the following conditions: 1) 96 o C for 0:20 2) 96 o C for 0:15 3) 72 o C for 2:20 4) Goto 2, 10 times 5) 96 o C for 0:20 6) 67 o C for 2:20 7) Goto 5, 25 times 8) 4 o C for ever Dilute the Hind/Eco PCR with 80 ml of MilliQ H 2 O. Go to Pcr 2. Load 6.5 ml of Ase pcr product on gel to visualize products. Go to Exonuclease step.

5 PCR2: This protocol uses Eppendorf HotMaster Taq. For one 96-well PCR plate prepare 2 tubes of the following: 1650 ml MilliQ H 2 O or similar PCR quality water 200 ml 10x HotMaster PCR Buffer 80 ml 10 mm dntps 3 ml 200 pmol LBb1 primer (3 ul of 11/19/02 stock) 3 ml 200 pmol AP2-C primer (4 ul of 11/01/02 stock) 5 ml HotMaster Taq Add 20 ml of PCR2 mix to each well of a 96-well PCR plate. Transfer 1.5 ml of diluted PCR1 product to each well. Cover with rubber mat and immediately load on MJ paused at the initial 96 o C step. Cycle on an MJ-200 Thermal Cycler with the following conditions: 1) 96 o C for 1:00 2) 94 o C for 0:20 3) 72 o C for 2:20 4) Goto 2, 5 times 5) 94 o C for 0:20 6) 67 o C for 0:20 7) 72 o C for 2:10 8) Goto 5, 23 times 9) 72 o C for 3:00 10) 4 o C hold Examine 3.5 ml of PCR2 product on a 1.0% agarose gel. IV. PCR Cleanup Exonuclease I (NEB # M0293S) is used to degrade the primers. For one 96-well PCR plate prepare the following: 275 ml MilliQ H 2 O or similar PCR quality water 30 ml 10x Sigma PCR Buffer 5 ml Exo I (10 U/ml) Add 3 ml of mix to each well of the plate. Add 20 ml of AseI Pcr product or 10 ml of Hind/Eco PCR2 product to each well. Incubate at 37 o C for 1.5 hours, then 80 o C for 20 minutes. Store at 4 o C. If the exo rxn is performed in a 384-well plate for the AseI products, an additional concentration step is required prior to precipitation. Place the plate in the speed-vac and put on high heat one hour. The liquid should be completely gone from the wells. Add 10

6 ml water to each reaction and let the DNA resuspend at least one half hour (overnight may be better) before precipitating. Store at 4 o C until ready to sequence. V. Cycle Sequencing Precipitate ml PCR product: Add 20 ml of EtOH/NaOAc mix (105 ml 95% EtOH, 7.5 ml 3M NaOAc ph 4.7, 2.5 ml H2O). Cover and mix thoroughly. Incubate at 80 o C for 15 minutes. Spin at 3000x g for 25 minutes. Remove supernatant by inverting plate on paper towel and gently flicking the plate. Wash pellets with 25 ml 70% EtOH. Spin 10 minutes at 2700x g. Dry the DNA by inverting the plates on a paper towel and pulse the centrifuge to 20x g. This protocol uses ABI Big Dye version 3.1 (# ) 5x Sequencing buffer is composed of 400 mm Tris-HCl ph 9.0 and 10 mm MgCl 2. For one 96-well PCR plate prepare the following: 700 ml MilliQ H 2 O or similar PCR quality water 200 ml 5x Sequencing Buffer 70 ml Big Dye v. 3 1 ml 200 pmol LBb1 primer (5 ml 40 pmol LBb1 primer) * * primer concentration can be increased or decreased as needed. Add 10 ml of mix to each well on the plate. Cycle on Gene Amp 9700 (Applied Biosystems) with heated lid using the following program: 1) 96 o C for 5:00 2) 96 o C for 0:25 3) 63 o C for 2:30 4) Goto 2, 47 times 5) 4 o C hold Precipitate the sequenced products using the EtOH/NaOAc protocol mentioned previously. To the dry sequence products add 10 ml of water. Load onto an ABI 3700 DNA sequencer.

7 REFERENCE José M. Alonso, Anna N. Stepanova, Thomas J. Leisse, Christopher J. Kim, Huaming Chen, Paul Shinn, Denise K. Stevenson, Justin Zimmerman, Pascual Barajas, Rosa Cheuk, Carmelita Gadrinab, Collen Heller, Albert Jeske, Eric Koesema, Cristina C. Meyers, Holly Parker, Lance Prednis, Yasser Ansari, Nathan Choy, Hashim Deen, Michael Geralt, Nisha Hazari, Emily Hom, Meagan Karnes, Celene Mulholland, Ral Ndubaku, Ian Schmidt, Plinio Guzman, Laura Aguilar-Henonin, Markus Schmid, Detlef Weigel, David E. Carter, Trudy Marchand, Eddy Risseeuw, Debra Brogden, Albana Zeko, William L. Crosby, Charles C. Berry, and Joseph R. Ecker (2003) Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana Science 301: